Source: CLINVAR ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		16 245 6 0.21 1 3.7E-03
CUI: C1858430
Disease: Death in infancy
Death in infancy 		6 0 4 0.20 0 0
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
Left ventricular noncompaction cardiomyopathy 		7 14 4 0.19 2 5.1E-02
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		3 0 3 0.17 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		3 0 3 0.17 0 0
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		3 0 3 0.17 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		5 24 3 0.15 1 2.0E-02
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		5 0 3 0.15 0 0
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		5 0 3 0.15 0 0
CUI: C1836906
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 		5 61 3 0.15 2 2.3E-02
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1 		5 73 3 0.15 1 1.0E-02
CUI: C0039070
Disease: Syncope
Syncope 		8 0 3 0.13 0 0
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		8 0 3 0.13 0 0
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S 		9 0 3 0.12 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		10 0 3 0.12 0 0
CUI: C0349788
Disease: Arrhythmogenic Right Ventricular Dysplasia
Arrhythmogenic Right Ventricular Dysplasia 		11 108 3 0.12 4 3.1E-02
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		2 0 2 0.11 0 0
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		2 3 2 0.11 1 3.4E-02
CUI: C1879286
Disease: Hereditary bundle branch system defect
Hereditary bundle branch system defect 		2 0 2 0.11 0 0
CUI: C3276240
Disease: LONG QT SYNDROME 2/3, DIGENIC
LONG QT SYNDROME 2/3, DIGENIC 		2 0 2 0.11 0 0
CUI: C3277700
Disease: LONG QT SYNDROME 1/2, DIGENIC (disorder)
LONG QT SYNDROME 1/2, DIGENIC (disorder) 		2 0 2 0.11 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		45 172 6 0.11 1 5.1E-03
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		3 0 2 0.11 0 0
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2 		3 0 2 0.11 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		14 0 3 0.10 0 0